Prostate cancer anticen-3 (PCA-3) and TMPRSS2-ERG (T2-ERG) score changes during initiation of androgen deprivation theray (ADT) with triptorelin 22.5 mg in patients with advanced prostate cancer (PCA): a phase II, single arm multicenter study - TRIPTOCARE

Ipsen Pharma S.A.S.0 sites315 target enrollmentNovember 9, 2010

Overview

No summary available.

Registry

who.int

Start Date

November 9, 2010

End Date

TBD

Last Updated

13 years ago

Study Type

Interventional clinical trial of medicinal product

Sex

Male

Sponsor

Ipsen Pharma S.A.S.

•All patients must fulfil the following: Patient must give written (personally signed and dated) informed consent before completing any study\-related procedure. Patient must be 18 years old or over. Patient must have a histologically confirmed, locally advanced or metastatic prostate cancer, and be na?ve to androgen deprivation therapy, and be candidate for hormonal treatment. Patient must have an estimated survival time of at least twelve months according to the investigator s assessment. Patient must have a performance status score \= 2 according to the WHO criteria.
•Are the trial subjects under 18? no
•Number of subjects for this age range:
•F.1\.2 Adults (18\-64 years) yes
•F.1\.2\.1 Number of subjects for this age range
•F.1\.3 Elderly (\>\=65 years) yes
•F.1\.3\.1 Number of subjects for this age range

•Patients will not be included in the study if: The patient with risk of a serious complication in the case of tumour flare (vertebral metastases threatening spinal cord compression or significant obstructive uropathy). The patient has had previous surgical castration. The patient has had previous or has planned curative prostate cancer therapy (radiation/surgery). The patient has had previous hormone therapy (GnRH analogues, estrogens or anti\-androgens). The patient is, in the opinion of the investigator, unable to comply fully with the protocol and the study instructions, or presents any concomitant condition which could compromise the objectives of the study and/or preclude the protocol\-defined procedures (e.g. severe medical conditions, brain metastasis, psychiatric disorders, active or uncontrolled infection, known pituitary disease). Patient who have received investigational drug or treatment within 30 days prior to study entry or will require a concurrent treatment with any other experimental drugs or treatments. Diagnosis of any other cancer without a history of stability/remission within five years of screening, with the exception of non\-metatastic basal and/or squamous cell carcinoma of the skin. Known hypersensitivity to triptorelin, GnRH, other GnRH agonist analogues or analogues to any excipients of the IMP